As a Class II or Class III medical device, the sterilizer must adhere to strict regulatory frameworks. Ensure the supplier provides ISO 13485 certification for medical device quality management systems. For the European market, CE marking (under MDR 2017/745) is essential, while for the US, FDA 510(k) clearance is required. Furthermore, the equipment should comply with EN 14937, which specifies the general requirements for the characterization of a sterilizing agent and the development, validation, and routine control of a sterilization process.